BD Preset Eclipse Arterial Blood Collection SyringeRecalls & reported problems across all models
Becton, Dickinson U.K. Limited · 3 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 278
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls
- 0
We found 3 models of BD Preset Eclipse Arterial Blood Collection Syringe by Becton, Dickinson U.K. Limited in the FDA's device registry (GUDID). Together they are named in 278 adverse event reports in the FDA's MAUDE database, received between Aug 28, 2018 and Sep 28, 2026 — classified as 3 injuries, 275 malfunctions.
The most frequently reported specific device problem is “Leak/Splash” (136 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported BD Preset Eclipse Arterial Blood Collection Syringe problems
Device problems
- Leak/Splash136
- Device Contamination with Chemical or Other Material42
- Volume Accuracy Problem26
- Device Markings/Labelling Problem12
- Packaging Problem10
- Component Missing8
- Fluid/Blood Leak7
- Coagulation in Device or Device Ingredient6
Patient problems
- No Clinical Signs, Symptoms or Conditions271
- No Known Impact Or Consequence To Patient4
- Needle Stick/Puncture3
BD Preset Eclipse Arterial Blood Collection Syringe models
3 models, most reported first. Each model has its own page with its reports, recalls and device details.
- BD Preset™ Eclipse™ Arterial Blood Collection Syringe 364390Tubes, vials, systems, serum separators, blood collection192 reports
- BD Preset™ Eclipse™ Arterial Blood Collection Syringe 364391Tubes, vials, systems, serum separators, blood collection47 reports
- BD Preset™ Eclipse™ Arterial Blood Collection Syringe 364389Tubes, vials, systems, serum separators, blood collection39 reports
Recent BD Preset Eclipse Arterial Blood Collection Syringe adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 28, 2026Device Contamination with Chemical or Other Material
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50915165 ↗MalfunctionSep 16, 2026Device Contamination with Chemical or Other Material
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50793757 ↗MalfunctionSep 15, 2026Device Contamination with Chemical or Other Material
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50777684 ↗MalfunctionSep 8, 2026Device Contamination with Chemical or Other Material
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50676778 ↗MalfunctionMay 28, 2026Fluid/Blood Leak
IT WAS REPORTED WHILE USING BD PRESET¿ ECLIPSE¿ ARTERIAL BLOOD COLLECTION SYRINGE, THE CAP HAD NOT BEEN SCREWED ON TIGHTLY ENOUGH RESULTING IN SAMPLE LEAKAGE. REPEAT COLLECTION OCCURRED. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25319053 ↗MalfunctionMay 21, 2026Fluid/Blood Leak
IT WAS REPORTED WHILE USING BD PRESET¿ ECLIPSE¿ ARTERIAL BLOOD COLLECTION SYRINGE, BLOOD LEAKED PAST THE PLUNGER OF FIVE (5) DEVICES. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25247326 ↗MalfunctionMay 21, 2026Device Contamination with Chemical or Other Material
IT WAS REPORTED WHILE USING BD PRESET¿ ECLIPSE¿, A FOREIGN OBJECT WAS SEEN ON THE PLUNGER OF ONE DEVICE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25242683 ↗MalfunctionMay 21, 2026Device Contamination with Chemical or Other Material
IT WAS REPORTED PRIOR TO USING BD PRESET¿ ECLIPSE¿ ARTERIAL BLOOD COLLECTION SYRINGE, ONE DEVICE CONTAINED FOREIGN MATTER ON THE PLUNGER. THERE WAS NO HEALTH IMPACT OR CONSEQUENCES REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25242251 ↗MalfunctionMay 18, 2026Difficult or Delayed Activation
IT WAS REPORTED WHILE USING BD PRESET¿ ECLIPSE¿ ARTERIAL BLOOD COLLECTION SYRINGE, THE LOCKING MECHANISM BECAME UNUSABLE ON ONE DEVICE AND TESTING HAD TO BE PERFORMED BY MANUALLY REMOVING THE SAFETY DEVICE. THERE WAS NO HEALTH IMPACT OR CONSEQUENCES REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25210824 ↗MalfunctionMay 15, 2026Missing Information
IT WAS REPORTED THAT BEFORE USAGE BD PRESET¿ ECLIPSE¿ ARTERIAL BLOOD COLLECTION SYRINGE, VOLUMETRIC MARKING WAS MISSING ON 1 DEVICE. NO ADVERSE IMPACT WAS REPORTED REGARDING PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25191205 ↗MalfunctionMay 14, 2026Device Contamination with Chemical or Other Material
IT WAS REPORTED PRIOR TO USING BD PRESET¿ ECLIPSE¿ ARTERIAL BLOOD COLLECTION SYRINGE, FOREIGN MATTER WAS OBSERVED IN 8 DEVICE PACKAGES. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25167070 ↗MalfunctionMay 4, 2026Device Contamination with Chemical or Other Material
IT WAS REPORTED WHILE USING BD PRESET¿ ECLIPSE¿ ARTERIAL BLOOD COLLECTION SYRINGE, A HAIR WAS DISCOVERED INSIDE THE NEEDLE HUB OF ONE DEVICE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25073819 ↗MalfunctionMay 4, 2026Device Markings/Labelling Problem
IT WAS REPORTED THAT PRIOR TO USING BD PRESET¿ ECLIPSE¿ ARTERIAL BLOOD COLLECTION SYRINGE, ONE SYRINGE WAS MISSING THE SCALE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25073375 ↗MalfunctionMay 1, 2026Device Contamination with Chemical or Other Material
IT WAS REPORTED WHILE USING BD PRESET¿ ECLIPSE¿ ARTERIAL BLOOD COLLECTION SYRINGE, FOREIGN MATTER WAS FOUND ON THE FLANGES OF ONE (1) DEVICE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25060123 ↗MalfunctionMay 1, 2026Short Fill
IT WAS REPORTED WHILE USING BD PRESET¿ ECLIPSE¿ ARTERIAL BLOOD COLLECTION SYRINGE, INSUFFICIENT BLOOD FLOW WAS SEEN WITH ONE DEVICE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25056172 ↗
Other Becton, Dickinson U.K. Limited products
All Becton, Dickinson U.K. Limited devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page